Literature DB >> 22437341

The collapsin response mediator protein 5 onconeural protein is expressed in Schwann cells under axonal signals and regulates axon-Schwann cell interactions.

Jean-Philippe Camdessanché1, Karine Ferraud, Nadia Boutahar, François Lassablière, Marie Mutter, Monique Touret, Pappachan Kolattukudy, Jérôme Honnorat, Jean-Christophe Antoine.   

Abstract

Collapsin response mediator protein 5 (CRMP5) is one of the rare peripheral nerve antigens that is a target of autoantibodies in a paraneoplastic peripheral neuropathy. The pattern of axonal and myelin alterations suggests that CRMP5 is involved in axon-Schwann cell interaction. We examined CRMP5 expression and function in primary cultures of Schwann cells and neurons and at various developmental and regenerating stages of rat sciatic nerve and in CRMP5-deficient mice in vivo. Collapsin response mediator protein 5 was strongly expressed during postnatal development and regeneration and decreased with myelination. It was mainly expressed by immature Schwann cells and persisted in Remak cells in the adult; however, a subpopulation of Schwann cells that were induced to myelinate also expressed CRMP5. We identified 2 axonal molecular cues regulating CRMP5 expression: human neuregulin type 1, which induces CRMP5 expression in immature and premyelinating Schwann cells, and cyclic adenosine monophosphate, which inhibits CRMP5 expression when Schwann cells begin myelination. Collapsin response mediator protein 5-deficient mice showed abnormal Schwann process extension resulting in abnormal cell-axon segregation, indicating that CRMP5 is involved in the morphologic adaptation of Schwann cells to surround axons. These results demonstrate the importance of CRMP5 in axon-Schwann cell cooperation during development and regeneration.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22437341     DOI: 10.1097/NEN.0b013e31824d1df2

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  4 in total

Review 1.  CRMPs: critical molecules for neurite morphogenesis and neuropsychiatric diseases.

Authors:  T T Quach; J Honnorat; P E Kolattukudy; R Khanna; A M Duchemin
Journal:  Mol Psychiatry       Date:  2015-06-16       Impact factor: 15.992

Review 2.  CRMPs Function in Neurons and Glial Cells: Potential Therapeutic Targets for Neurodegenerative Diseases and CNS Injury.

Authors:  Jun Nagai; Rina Baba; Toshio Ohshima
Journal:  Mol Neurobiol       Date:  2016-06-23       Impact factor: 5.590

3.  Treatment options in paraneoplastic disorders of the peripheral nervous system.

Authors:  Jean-Christophe Antoine; Jean-Philippe Camdessanché
Journal:  Curr Treat Options Neurol       Date:  2013-04       Impact factor: 3.598

4.  Insights into olfactory ensheathing cell development from a laser-microdissection and transcriptome-profiling approach.

Authors:  Surangi N Perera; Ruth M Williams; Rachel Lyne; Oliver Stubbs; Dennis P Buehler; Tatjana Sauka-Spengler; Masaharu Noda; Gos Micklem; E Michelle Southard-Smith; Clare V H Baker
Journal:  Glia       Date:  2020-08-28       Impact factor: 8.073

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.